Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K022740 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Datex-Ohmeda S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software... | 2 | 09/01/2009 |
FEI # 3005860720 GE Medical Systems Information Tecnology |
| Datex-Ohmeda S/5 Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software. ... | 2 | 09/01/2009 |
FEI # 3005860720 GE Medical Systems Information Tecnology |
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